A new terpene coumarin microbial transformed by Mucor polymorphosporus induces apoptosis of human gastric cancer cell line MGC-803

被引:0
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作者
Guangzhi Li
Junchi Wang
Xiaojin Li
Jianguo Xu
Zhao Zhang
Jianyong Si
机构
[1] Chinese Academy of Medical Sciences,Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Peking Union Medical College
[2] The Third Affiliated Hospital of Shenzhen University,Shenzhen Luohu People’s Hospital
[3] Xinjiang Institute of Chinese Materia Medica and Ethical Materia Medica,undefined
来源
Archives of Pharmacal Research | 2018年 / 41卷
关键词
Biotransformation; Terpene coumarin; Human gastric cancer MGC-803 cell line; Apoptosis;
D O I
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中图分类号
学科分类号
摘要
2′-Z auraptene (1) is a synthesized monoterpene coumarin with anticancer activity against human gastric cancer cells. In order to find new potential anticancer agent, Mucor polymorphosporus was used to transform cis-auraptene. Four new terpene coumarins with notable changes in the skeletal backbone, 2′-Z auraptene A-D (2–5), were obtained and evaluated for their antiproliferative effects against human normal gastric epithelium cells and human gastric cancer cells. These new compounds showed selective cytotoxic activity against MGC-803 cells with IC50 values from 0.78 ± 0.13 to 10.78 ± 1.83 μM and the therapeutic index could also be significantly improved (TI = 59.0) compared with that of 1 (TI = 5.5). The structures of these metabolites were elucidated through extensive spectroscopic methods, and the possible biotransformation pathway of 1 by Mucor polymorphosporus was also proposed. Furthermore, the mechanism of the antiproliferative effects against MGC-803 cells of the most potent compound, 2′-Z auraptene A (2), was characterized. Annexin V/PI staining and abnormal expression of apoptosis-related protein suggested that compound 2 induces apoptosis in gastric cancer MGC-803 cells. Therefore, it is possible that compound 2 has the potential to be applied in gastric cancer therapy.
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页码:646 / 654
页数:8
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